HS 293944 Norephedrine and its salts
Quick Answer: HS code 293944 specifically covers Norephedrine and its salts. Norephedrine, also known as phenylpropanolamine (PPA), is a sympathomimetic amine used as a stimulant, decongestant, and anorectic agent. Due to its chemical properties and potential for misuse, it is subject to strict regulatory controls in many countries. For importers and exporters, understanding these controls is paramount. Duty rates for this classification vary significantly. The United Kingdom and the European Union generally apply a 0.00% ad valorem duty rate. In contrast, the United States imposes a more complex duty structure, typically "Free" for certain origins, but can also be 15.4¢/kg + 59% ad valorem, depending on the specific product and country of origin. Importers must verify the exact duty rate and any applicable quotas or special provisions through the USITC Harmonized Tariff Schedule. Given its controlled substance status, meticulous documentation and adherence to national drug enforcement regulations are critical for compliance.
What Are the Import Duty Rates?
🇬🇧 United Kingdom
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 2939440000 | 0.00 % | — | — |
🇪🇺 European Union (TARIC)
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 2939440000 | 0.00 % | — | — |
🇺🇸 United States (HTSUS)
| Code | MFN | Preferential | Unit |
|---|---|---|---|
| 2939440000 | Free | — | ["kg"] |
Duty rates sourced from the USITC (US International Trade Commission) Harmonized Tariff Schedule (HTS) (accessed 2/22/2026), EU TARIC – DG TAXUD (Directorate-General for Taxation and Customs Union) (accessed 2/22/2026), and UK Trade Tariff – HMRC (His Majesty's Revenue and Customs) (accessed 2/22/2026).
Data compiled and presented by HSRates.
How Has Trade Volume Developed?
Trade Volume 2023
How to Classify This HS Code?
What products does HS 293944 cover?
This subheading covers Norephedrine and its salts, specifically referring to the chemical compound (1R,2S)-2-amino-1-phenylpropan-1-ol, also known as phenylpropanolamine (PPA) or cathine, and its various salt forms. As per the World Customs Organization (WCO) Harmonized System Nomenclature and further detailed in the USITC Harmonized Tariff Schedule (HTS) and EU TARIC, this classification is precise for the pure chemical substance and its derivatives formed through salt reactions. Norephedrine is a sympathomimetic amine, often used as a decongestant or anorectic, and its classification here reflects its specific chemical identity within the broader category of vegetable alkaloids and their derivatives.
What falls outside HS 293944?
The following products are excluded from HS 293944: preparations containing norephedrine but formulated for specific therapeutic or prophylactic uses, which would typically fall under Chapter 30, such as medicaments of heading 3004. For instance, a cough syrup containing norephedrine as an active ingredient would be classified under 3004, not 293944. Similarly, isomers of norephedrine that are not specifically norephedrine (e.g., pseudoephedrine, which has its own distinct subheading 293943) are also excluded. Mixtures of norephedrine with other substances, where the norephedrine is not the predominant character-imparting component, would also be classified elsewhere, often under Chapter 38 or 30 depending on their nature and use.
What are common classification mistakes for HS 293944?
A common error is misclassifying pharmaceutical preparations containing norephedrine directly under 293944 instead of Chapter 30. Importers often overlook Legal Note 1(a) to Chapter 30, which states that medicaments are classified in heading 3003 or 3004, even if they consist of unmixed products suitable for therapeutic or prophylactic uses. Another frequent mistake involves confusing norephedrine with its stereoisomers, such as pseudoephedrine (HS 293943), or other related sympathomimetic amines. Proper classification requires strict adherence to the chemical structure and identity, as per General Interpretative Rule (GRI) 1, which mandates classification according to the terms of the headings and any relative section or chapter notes.
How should importers classify products under HS 293944?
The correct procedure for classifying products under HS 293944 involves first verifying the exact chemical identity of the substance as Norephedrine or one of its salts, typically through a Certificate of Analysis (CoA) or Material Safety Data Sheet (MSDS). Importers and customs brokers must ensure the product is not a medicament or a preparation, as defined by Chapter 30 notes. If it is a pure chemical substance, GRI 1 directs classification to Heading 2939, then specifically to subheading 293944. For any doubt, consulting the WCO Explanatory Notes for Chapter 29 and obtaining a binding tariff information (BTI) decision from the relevant customs authority (e.g., CBP in the US, national customs in the EU) is highly recommended to ensure compliance and avoid potential penalties.
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FAQ
What are the Most Favored Nation (MFN) duty rates for HS code 2939.44 (Norephedrine and its salts) in key markets?
The MFN duty rates for HS 2939.44 vary by importing country. For example, the United States generally applies a 'Free' rate for products classified under 2939.44.00, as per the Harmonized Tariff Schedule of the United States (HTSUS). The European Union's TARIC database also indicates a '0.00 %' ad valorem duty rate for this heading. Importers should always consult the specific tariff schedule of the destination country, such as the USITC HTSUS, EU TARIC, or UK Trade Tariff, for the most current and authoritative rates.
What are the key classification criteria for 'Norephedrine and its salts' under HS 2939.44, and how is it distinguished from similar substances?
HS 2939.44 specifically covers 'Norephedrine and its salts.' Classification hinges on the chemical identity of the substance. Norephedrine (also known as Phenylpropanolamine or PPA) is an alkaloid. The WCO Explanatory Notes for Chapter 29 provide guidance on the chemical structure and properties of organic chemicals. Importers must ensure that the substance is chemically identified as norephedrine or one of its salts (e.g., norephedrine hydrochloride). This distinguishes it from other ephedrine-type alkaloids (like ephedrine or pseudoephedrine, classified elsewhere in 2939) based on their precise molecular structure and functional groups. Laboratory analysis and Certificates of Analysis (CoA) are crucial for accurate classification.
Are there any specific documentation requirements or regulatory controls for importing Norephedrine and its salts (HS 2939.44) due to its nature as a pharmaceutical precursor?
Yes, due to its potential use as a precursor in the illicit manufacture of controlled substances, Norephedrine (Phenylpropanolamine) is subject to strict regulatory controls in many countries. In the United States, it is regulated under the Combat Methamphetamine Epidemic Act of 2005 (CMEA) and is a List I chemical under the Drug Enforcement Administration (DEA). Importers typically require a DEA import permit, must register with the DEA, and comply with strict record-keeping requirements. Similarly, the European Union regulates it under Regulation (EC) No 273/2004 on drug precursors. Importers will need to provide end-use statements, import licenses, and comply with national competent authority requirements. Customs brokers must verify that all necessary permits and declarations are in place before importation.
Which preferential trade agreements might offer duty-free treatment for HS 2939.44, and what are the origin requirements?
Given that the MFN duty rate for HS 2939.44 is often 'Free' or '0.00 %' in major markets like the US and EU, preferential trade agreements (PTAs) may not offer additional duty savings for this specific code. However, PTAs can still be relevant for other reasons (e.g., simplified customs procedures). If a duty were applicable, agreements such as the USMCA (United States-Mexico-Canada Agreement), EU's various Free Trade Agreements (e.g., with Japan, South Korea), or the UK's trade agreements could potentially offer preferential duty treatment. To qualify, the goods must meet the specific Rules of Origin (ROO) outlined in the respective agreement. Typically, this involves satisfying a change in tariff classification (CTC), a regional value content (RVC) requirement, or a specific processing rule, and providing a valid Certificate of Origin or origin declaration.